The serotonin signaling system plays
a crucial role in
regulating
the ontogeny of crustaceans. Here, we describe the effects of different
concentrations of the 5-hydroxytryptamine 1A receptor antagonist (WAY-100635)
on the induced antipredation (Rhodeus ocellatus as the predator), morphological, behavioral, and life-history defenses
of Daphnia magna and use transcriptomics
to analyze the underlying molecular mechanisms. Our results indicate
that exposure to WAY-100635 leads to changes in the expression of
different defensive traits in D. magna when faced with fish predation risks. Specifically, as the length
of exposure to WAY-100635 increases, high concentrations of WAY-100635
inhibit defensive responses associated with morphological and reproductive
activities but promote the immediate negative phototactic behavioral
defense of D. magna. This change is
related to the underlying mechanism through which WAY-100635 interferes
with gene expression of G-protein-coupled GABA receptors by affecting
GABBR1 but promotes serotonin receptor signaling and ecdysteroid signaling
pathways. In addition, we also find for the first time that fish kairomone
can significantly activate the HIF-1α signaling pathway, which
may lead to an increase in the rate of immediate movement. These results
can help assess the potential impacts of serotonin-disrupting psychotropic
drugs on zooplankton in aquatic ecosystems.